Genetic Modification, although a newly developing field of scientific study, has become a pertinent topic of ethical debate due to rapid advancements in the technology. Therapeutic Human Genome Editing was first discussed in the 1970s due to its invention. Modern gene editing called CRISPR facilitates much more complex gene modification, allowing for its applications to become widespread, including curing sickle cell anemia, immunodeficiency, retinal and dermatologic disorders, preventing cancer, slowing the propagation of cancer, and deceleration of the aging process (Joseph AM et al.)…